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40. Meet an Expert: Wes Michael, President at Rare Patient Voice

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Manage episode 331976170 series 3001364
Innhold levert av Shivani Vyas. Alt podcastinnhold, inkludert episoder, grafikk og podcastbeskrivelser, lastes opp og leveres direkte av Shivani Vyas eller deres podcastplattformpartner. Hvis du tror at noen bruker det opphavsrettsbeskyttede verket ditt uten din tillatelse, kan du følge prosessen skissert her https://no.player.fm/legal.

Show Notes:

In this episode, I chat with Wes Michael, President at Rare Patient Voice.

Wes Michael, President and Founder of Rare Patient Voice, has been involved in rare and orphan diseases since 1998, interviewing and surveying patients, caregivers, physicians, nurses and advocacy leaders. Wes has more than 40 years experience in marketing research, and more than 20 years in healthcare marketing research.

Rare Patient Voice, LLC provides patients and caregivers with rare diseases an opportunity to voice their opinions through surveys and interviews to improve medical products and services.

While Rare Patient Voice started by focusing on rare diseases, they now welcome patients and caregivers with all medical conditions.

Rare Patient Voice takes an active approach to meet patients at conferences and events. Their phone is always open to members. The more they can engage with patients, the more they can advocate for them and help their voices be heard.

Explore more!

Website: https://rarepatientvoice.com/

LinkedIn: https://www.linkedin.com/company/rare-patient-voice/

See you all next week!

- Shivani Vyas ☺

@raredisorderpod on IG, FB, & Twitter, The Rare Disorder Podcast on LinkedIn
https://linktr.ee/theraredisorderpodcast

--- Support this podcast: https://podcasters.spotify.com/pod/show/theraredisorderpodcast/support
  continue reading

42 episoder

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iconDel
 
Manage episode 331976170 series 3001364
Innhold levert av Shivani Vyas. Alt podcastinnhold, inkludert episoder, grafikk og podcastbeskrivelser, lastes opp og leveres direkte av Shivani Vyas eller deres podcastplattformpartner. Hvis du tror at noen bruker det opphavsrettsbeskyttede verket ditt uten din tillatelse, kan du følge prosessen skissert her https://no.player.fm/legal.

Show Notes:

In this episode, I chat with Wes Michael, President at Rare Patient Voice.

Wes Michael, President and Founder of Rare Patient Voice, has been involved in rare and orphan diseases since 1998, interviewing and surveying patients, caregivers, physicians, nurses and advocacy leaders. Wes has more than 40 years experience in marketing research, and more than 20 years in healthcare marketing research.

Rare Patient Voice, LLC provides patients and caregivers with rare diseases an opportunity to voice their opinions through surveys and interviews to improve medical products and services.

While Rare Patient Voice started by focusing on rare diseases, they now welcome patients and caregivers with all medical conditions.

Rare Patient Voice takes an active approach to meet patients at conferences and events. Their phone is always open to members. The more they can engage with patients, the more they can advocate for them and help their voices be heard.

Explore more!

Website: https://rarepatientvoice.com/

LinkedIn: https://www.linkedin.com/company/rare-patient-voice/

See you all next week!

- Shivani Vyas ☺

@raredisorderpod on IG, FB, & Twitter, The Rare Disorder Podcast on LinkedIn
https://linktr.ee/theraredisorderpodcast

--- Support this podcast: https://podcasters.spotify.com/pod/show/theraredisorderpodcast/support
  continue reading

42 episoder

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